AMLODIPINE BESYLATE
- Product NDC
- 45865-810
- 11-digit product format
- 458650810
- Labeler code
- 45865
- Product ID
- 45865-810_7dc972ad-2867-39a9-e053-2a91aa0a62ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA077073
- Marketing category
- ANDA
- Marketing start
- 2007-09-26
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-810-49 | AMLODIPINE BESYLATE | 100 in 1 BOTTLE | TABLET | 100 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-810 | AMLODIPINE BESYLATE TABLET [MEDSOURCE PHARMACEUTICALS] | 8 | Legacy NDC, 1 package rows | 20181225_7dc972ad-2866-39a9-e053-2a91aa0a62ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-810-49 | 45865081049 | 100 in 1 BOTTLE | Historical |